| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5287591 | Tetrahedron Letters | 2007 | 5 Pages |
Abstract
A regioselective synthesis of 2,4,6-trisubstituted pyridine is described starting from 2,6-dibromo-4-nitropyridine. All three different regioisomers of the 2,4,6-triamino substituted pyridine have been synthesized in four to five steps. The method described is a general route to unsymmetrical 2,4,6-trisubstituted amino pyridines.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Rupa Shetty, Duyan Nguyen, Dietmar Flubacher, Franziska Ruggle, Andreas Schumacher, Martha Kelly, Enrique Michelotti,